Canonical Allele Identifier: CA1457431744
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52033514T= , CM000666.2:g.52033514T= GRCh38
NC_000004.11:g.52899680T= , CM000666.1:g.52899680T= GRCh37
NC_000004.10:g.52594437T= NCBI36
NG_008891.1:g.9806A= , LRG_204:g.9806A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.160A= MANE Select ENSP00000370839.6:p.Lys54=
ENST00000381431.9:c.160A= ENSP00000370839.5:p.Lys54=
ENST00000506357.5:c.146A=
ENST00000514133.1:c.127A= ENSP00000425818.1:p.Lys43=
NM_000232.4:c.160A= , LRG_204t1:c.160A= NP_000223.1:p.Lys54=
XM_006714049.2:c.-248A= XP_006714112.1:n.-248A=
XM_011534403.1:c.34-3651A= XP_011532705.1:n.34-3651A=
XM_011534404.1:c.-225A= XP_011532706.1:n.-225A=
NM_000232.5:c.160A= MANE Select NP_000223.1:p.Lys54=